Stephen Archacki

Stephen Archacki, Qiuyun Chen, Chengqi Xu, 2021, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery disease.

E. Topol, George O. Angheloiu, Stephen Archacki, 2012, Human molecular genetics.

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.

Changzheng Huang, Qing Wang, Mugen Liu, 2012, Gene.

Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis.

Changzheng Huang, Mugen Liu, Stephen Archacki, 2016, Clinica chimica acta; international journal of clinical chemistry.

Proteomic approach to coronary atherosclerosis shows ferritin light chain as a significant marker: evidence consistent with iron hypothesis in atherosclerosis.

E. Topol, Shaoqi Rao, George O. Angheloiu, 2003, Physiological genomics.

Splice variants of lncRNA RNA ANRIL exert opposing effects on endothelial cell activities associated with coronary artery disease

Fan Wang, Stephen Archacki, Qiuyun Chen, 2020, RNA biology.

MOLECULAR IDENTIFICATION OF NOVEL GENES ASSOCIATED WITH ATHEROSCLEROSIS

Stephen Archacki, 2011 .

Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome‐Wide Association Studies

K. Rawlik, A. Tenesa, Chunyan Luo, 2020, Journal of the American Heart Association.

Expression profiling of cardiovascular disease

Stephen Archacki, Qing Wang, 2004, Human Genomics.

Correction: Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes.

Fan Wang, Stephen Archacki, Qiuyun Chen, 2019, The Journal of Biological Chemistry.

Long noncoding RNA ANRIL regulates endothelial cell activities associated with coronary artery disease by up-regulating CLIP1, EZR, and LYVE1 genes

Fan Wang, Stephen Archacki, Qiuyun Chen, 2019, The Journal of Biological Chemistry.

Analysis of causal effect of APOA5 variants on premature coronary artery disease

E. Topol, S. Ellis, J. Barnard, 2018, Annals of human genetics.

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

Fei Liu, Y. Liu, Mugen Liu, 2016, Molecular vision.

Microarray analysis of cardiovascular diseases.

Stephen Archacki, Stephen R Archacki, Qing K Wang, 2006, Methods in molecular medicine.

Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

Fei Liu, Tao Jiang, Mugen Liu, 2018, Human Genetics.

A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery Disease and Myocardial Infarction in the LRP8 Gene

E. Topol, D. Girelli, O. Olivieri, 2014, Circulation. Cardiovascular genetics.

, Gene LRP 8 Disease and Myocardial Infarction in the A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery

E. Topol, D. Girelli, O. Olivieri, 2014 .

Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy

Fei Liu, Tao Jiang, Mugen Liu, 2018, Human Genetics.

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.

Changzheng Huang, Qing Wang, Mugen Liu, 2012, Gene.